Directions
Instill one or two drops in the affected eye(s) as needed.
Hylatears Liquid
FDA Label NDC 72094-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Hyalogic Llc for the product Hylatears (NDC 72094-001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding principal display panel, directions, otc - purpose, keep out of reach, warnings, inactive ingredient, otc - active ingredient, inidication and use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose (Purpose)
Purpose: Lubricant
Keep Out Of Reach
Keep out of reach of children
Warnings
Warnings (Warnings)
If you are pregnant, nursing, trying to conceive, taking any medications, or have a medical condition, please consult your healthcare practitioner before using this product.
Stop use and ask a doctor if: You experience eye pain, changes in vision, continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours.
Do not use if solution changes color or becomes cloudy.
If swallowed, get medical help or contact a Poison Control Center right away.
Keep out of reach of children.
Inactive Ingredient
Inactive Ingredients:
Water, sodium chloride, sodium hyaluron-ate, potassium chloride, sodium phosphate dibasic, sodium phosphate monobasic, benzyl alcohol.
Otc - Active Ingredient
Hypromellose 0.3% Lubricant
Inidication And Use
For the temporary relief of burning, irritaiton and discomofrt due to drynes of the eye or exposure to wind and sun,. May be uysed as a protectant against further irritation
* Please review the disclaimer below.
